Bromide

Bromide

SCHEMBL10972264

C#CCN(C=Cc1sc2ccccc2[n+]1C)c1ccccc1.[Br-]

nearest known ligand 0.47

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

ACHECHKACHRM1CHRM2CHRM3CHRM4CHRM5CHRNA1CHRNB1CHRNDCHRNECHRNGHRH2OPRM1

The experimentally established mechanism targets of Bromide. The predicted profile below is derived independently by chemical similarity — agreement is a validation signal, a miss is honest.

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
▸ INSR P06213 10/20 0.47
▸ ADRB2 P07550 2/20 0.46
▸ ADRB1 P08588 1/20 0.46
▸ MAPT P10636 4/20 0.42
▸ HTT P42858 3/20 0.42
▸ POLB P06746 2/20 0.42
▸ RAB9A P51151 2/20 0.42
▸ NSD2 O96028 1/20 0.42
▸ MAPK1 P28482 1/20 0.42
▸ NPSR1 Q6W5P4 1/20 0.42
▸ L3MBTL1 Q9Y468 1/20 0.42
▸ MEN1 O00255 2/20 0.39
▸ KMT2A Q03164 2/20 0.39
▸ ALDH1A1 P00352 1/20 0.39
▸ CYP1A2 P05177 1/20 0.39
▸ CYP3A4 P08684 1/20 0.39
▸ CYP2D6 P10635 1/20 0.39
▸ CYP2C9 P11712 1/20 0.39
▸ ALOX12 P18054 1/20 0.39
▸ CYP2C19 P33261 1/20 0.39

Click a target to see other patent compounds predicted against it — the reverse direction, in place.

Similar compounds — the chemically nearest patent molecules

Nearest neighbours by Morgan-fingerprint cosine across the patent-compound collection, with each neighbour's top predicted target and the predicted targets it shares with this molecule.

Compoundsimilaritytop predictedshared targets
Bromide SCHEMBL10972261 1.00 INSR (0.47) INSRADRB2ADRB1MAPTHTT
SCHEMBL10974922 0.99 INSR (0.48) INSRADRB2ADRB1MAPTHTT
Bromide SCHEMBL11285087 0.80 ADRB2 (0.40) INSRADRB2ADRB1MAPTHTT
SCHEMBL10971186 0.76 INSR (0.59) INSRADRB2ADRB1MAPTHTT
SCHEMBL10971188 0.76 INSR (0.59) INSRADRB2ADRB1MAPTHTT
Hydrochloric Acid SCHEMBL11516421 0.71 INSR (0.60) INSRADRB2ADRB1MAPTHTT
Hydrochloric Acid SCHEMBL11516423 0.71 INSR (0.60) INSRADRB2ADRB1MAPTHTT
SCHEMBL11290414 0.71 ALDH1A1 (0.39) INSRADRB2ADRB1MAPTHTT
SCHEMBL11290416 0.71 ALDH1A1 (0.39) INSRADRB2ADRB1MAPTHTT
SCHEMBL30924933 0.71 MAPT (0.63) INSRADRB2ADRB1MAPTHTT

Similarity is cosine over the 2,048-bit Morgan fingerprint (≈ Tanimoto). Identical fingerprints score 1.00.

Patent provenance — the patents this molecule appears in, and who filed them

Claimed or disclosed in 4 patents. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-0050558-A2 Photographic emulsions and elements capable of forming direct-positive images EASTMAN KODAK COMPANY (a New Jersey corporation) (US) 1982-04-28 — — EP claimed
EP-0050558-B1 PHOTOGRAPHIC EMULSIONS AND ELEMENTS CAPABLE OF FORMING DIRECT-POSITIVE IMAGES EASTMAN KODAK COMPANY (a New Jersey corporation) (US) 1985-07-17 — — EP disclosed
EP-0050558-A2 Photographic emulsions and elements capable of forming direct-positive images EASTMAN KODAK COMPANY (a New Jersey corporation) (US) 1982-04-28 — — EP disclosed
US-4306016-A HETEROCYCLIC CYANINE DYE-LIKE NUCLEATING AGENTS EASTMAN KODAK COMPANY (US) 1981-12-15 — — US disclosed
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